1 ; R. balochistanensis has virtually complete
fore- and hind limbs.
2 Eml5 transcripts can be detected in
fore- and hindbrain structures from embryonic day 13 onw
3 expanded structures in the fat pads of their
fore- and hindfeet, but for three centuries these have b
4 ouse cerebellum, midbrain, nasal process and
fore- and hindlimb buds.
5 Using Tbx5 and Tbx4 as
fore- and hindlimb field markers, respectively, we have
6 Furthermore, we found that both
fore- and hindlimb fields arise gradually during gastrul
7 rebro-olivocerebellar paths originating from
fore- and hindlimb motor cortex has implications for the
8 creases in horizontal bar test catalepsy and
fore- and hindlimb paw retraction latencies.
9 ud occurs in the anterior mesenchyme of both
fore- and hindlimb.
10 specify the differential development of the
fore- and hindlimbs are unknown.
11 ages, pectoral and pelvic fins in fishes and
fore- and hindlimbs in tetrapods.
12 th and a 30% decrease in inflammation in the
fore- and hindlimbs of mdx mice.
13 tensive anterior digit abnormalities of both
fore- and hindlimbs, while all double Bmp4(tm1); Alx4(tm
14 distinct structures, such as the vertebrate
fore- and hindlimbs.
15 tal digit duplications were seen in both the
fore- and hindlimbs.
16 birth, despite the complete absence of both
fore- and hindlimbs.
17 so exhibit syndactyly (digit fusions) of the
fore- and hindlimbs.
18 phrenic nerve, and the dorsal motor nerve in
fore- and hindlimbs.
19 Fore- and hindpaw withdrawal latencies from a 30 degrees
20 a-receptors, in adjacent coronal sections in
fore- and midbrain and in sagittal sections, were labell
21 O binding to mu-opioid receptors in selected
fore- and midbrain regions of chickens subject to varyin
22 tivity was evident in several regions of the
fore- and midbrain, in support of putative homologies to
23 thalamus at the expense of the ZLI and other
fore- and/or mid-brain regions.
24 ssion of both genes was found in adult mouse
fore- but not mid- or hindbrain.
25 ru imposed strong balancing selection on the
Fore, essentially eliminating PRNP 129 homozygotes.
26 isorder characterised predominantly by upper(
fore) limb defects and heart abnormalities.
27 dermal cell lineages and a gut consisting of
fore-, mid- and hindgut.
28 ormation of large hemorrhages throughout the
fore-, mid-, and hindbrain by E11.5.
29 nd oligodendrocytes, which populate the host
fore-, mid-, and hindbrain.
30 pattern is formed from three broad domains:
fore-, mid-, and hindgut that have distinct functional,
31 l breast milk samples, with a gradient from "
fore" milk to "hind" milk.
32 Electrical stimulation of the ipsilateral
fore- or hindimbs or somatotopically corresponding parts
33 ssion domains in the heart and the exclusive
fore- or hindlimb expression of Tbx5 and Tbx4, respectiv
34 o-Ruby or Fluoro-Emerald) were made into the
fore- or hindlimb parts of the motor cortex where stimul
35 ding (spino-olivocerebellar) paths targeting
fore- or hindlimb-receiving parts of the C1 zone.
36 are, in marked contrast to younger unexposed
Fore, predominantly PRNP 129 heterozygotes.
37 isms of aggregate formation have come to the
fore, suggesting that nucleation-dependent aggregation m
38 quantum simulators has recently come to the
fore: they generally require less memory than their clas
39 usly shown that combining Fourier rebinning (
FORE) with 2-dimensional (2D) statistical image reconstr